HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → Benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | Benzhydryl 7-formamido-3-methylenecepham-4-carboxylate | HCID 86744523 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate | HCID 88528581 | — |
Reaction Steps
A solution of benzhydryl 7-formamido-3-methylenecepham-4-carboxylate (40.8 g) in methylene chloride (300 ml) and methanol (1.2 l) was cooled at -74° C. in a dry ice-acetone bath. A theoretical amount of ozone was blown through the solution at -74° C. for 10 minutes with stirring, and nitrogen gas was blown through the solution at -74° C. for 10 minutes Dimethyl sulfide (20 ml) was added to the solution at -74° C. The mixture was slowly warmed to ambient temperature and evaporated in vacuo. The residue was subjected to column chromatography on silica gel and eluted with ethyl acetate. The eluent was evaporated in vacuo to give benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate (34.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985555 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-0d2a2342ac7d4f258d81df17c3e3f13e |
| Source note | uspto-grants-1991_01 |